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PRMT5 regulates alternative splicing of TCF3 under hypoxia to promote EMT and invasion in breast cancer
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PRMT5 regulates alternative splicing of TCF3 under hypoxia to promote EMT and invasion in breast cancer
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Journal Article
PRMT5 regulates alternative splicing of TCF3 under hypoxia to promote EMT and invasion in breast cancer
2025
Overview
Tumor hypoxia induced alterations in the epigenetic landscape and alternative splicing influence cellular adaptations. PRMT5 is a type II protein arginine methyltransferase that regulates several tumorigenic events in many cancer types. However, the regulation of PRMT5 and its direct implication on aberrant alternative splicing under hypoxia remains unexplored. In this study, we observed hypoxia-induced upregulation of PRMT5 via the CTCF in human breast cancer cells. Further, PRMT5-mediated symmetric arginine dimethylation H4R3me2s and H3R8me2s directly regulated the alternative splicing of TCF3 . Under hypoxia, PRMT5-mediated histone dimethylation at the intronic conserved region (ICR) present between TCF3 exon 18a and exon 18b recruits DNMT3A, resulting in DNA methylation. DNA methylation at the TCF3 -ICR is recognized and bound by MeCP2 resulting in RNA-Pol II pausing, promoting the recruitment of the negative splicing factor PTBP1 to the splicing locus of TCF3 pre-mRNA. PTBP1 promotes the exclusion of exon 18a which results in the production of the pro-invasive TCF3-18B (E47) isoform which promotes EMT and invasion of breast cancer cells under hypoxia. Collectively, our results indicate PRMT5-mediated symmetric arginine dimethylation of histones regulates alternative splicing of TCF3 gene thereby enhancing EMT and invasion in breast cancer hypoxia.
Publisher
Public Library of Science,PLOS,Public Library of Science (PLoS)
Subject
Alternative Splicing - genetics
/ Basic Helix-Loop-Helix Transcription Factors - genetics
/ Basic Helix-Loop-Helix Transcription Factors - metabolism
/ Breast Neoplasms - metabolism
/ Breast Neoplasms - pathology
/ Cancer
/ Epithelial-Mesenchymal Transition - genetics
/ Exons
/ Female
/ Gene Expression Regulation, Neoplastic
/ Humans
/ Medicine and Health Sciences
/ Protein-Arginine N-Methyltransferases - genetics
/ Protein-Arginine N-Methyltransferases - metabolism
/ Repressor Proteins - metabolism
